# FDA Inspection 842372 - Claritec Company - July 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/claritec-company/699aab96-2fc4-4022-b7d4-5aa643b0fdc2
Source feed: FDA_Inspections

> FDA Inspection 842372 for Claritec Company on July 25, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 842372
- Company Name: Claritec Company
- Inspection Date: 2013-07-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 842372 - 2013-07-25](https://www.keypedia.com/records/fda_inspections/claritec-company/1c42ce66-57eb-499d-83fb-3996cb407853)
- [FDA Inspection 659539 - 2010-04-26](https://www.keypedia.com/records/fda_inspections/claritec-company/24fac784-0a9d-4c89-af7f-0e7d2927e0c7)

Company: https://www.keypedia.com/companies/claritec-company/bda8f891-0de9-4504-bcfd-b3d617c3f17b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7